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Xenical

Clinical Pharmacology
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Clinical Pharmacology

In the XENDOS trial, in the overall population, orlistat delayed the onset of type 2 diabetes such that at the end of four years of treatment the cumulative incidence rate of diabetes was 8.3% for the placebo group compared to 5.5% for the orlistat group, p=0.01 (see Table 6 ). This finding was driven by a statistically-significant reduction in the incidence of developing type 2 diabetes in those patients who had impaired glucose tolerance at baseline (Table 6 and Figure 2). Orlistat did not reduce the risk for the development of diabetes in patients with normal glucose tolerance at baseline.

The effect of XENICAL to delay the onset of type 2 diabetes in obese patients with IGT is presumably due to weight loss, and not to any independent effects of the drug on glucose or insulin metabolism. The effect of orlistat on weight loss is adjunctive to diet and exercise.

Table 6: Incidence Rate of Diabetes at Year 4 by OGTT Status at Baseline*

OGTT at baseline Normal Impaired All
Treatment Placebo Orlistat Placebo Orlistat Placebo Orlistat
Number of patients* 1148 1235 324 337 1472 1572
# pts developing diabetes
Life table rate
Observed percent
16
2.1%
1.4%
21
1.7%
1.7%
62
27.2%
19.1%
48
18.7%
14.2%
78
8.3%
5.3%
69
5.5%
4.4%
Absolute risk reduction
Life table
Observed
0.4%
-0.3%
8.5%
4.9%
2.8%
0.9%
Relative risk reduction†† 8% 42% 34%
p-value 0.79 < 0.01 0.01
*Based on patients with a baseline and at least one follow-up OGTT measurement
Rate adjusted for dropouts
††Computed as (1- hazard ratio)

Figure 2: Percentage of Patients Without Diabetes Over Time

Percentage of Patients Without Diabetes Over Time - illustration

Pediatric Clinical Studies

The effects of XENICAL on body mass index (BMI) and weight loss were assessed in a 54-week multicenter, double-blind, placebo-controlled study in 539 obese adolescents (357 receiving XENICAL 120 mg three times a day, 182 receiving placebo), aged 12 to 16 years. All study participants had a baseline BMI that was 2 units greater than the US weighted mean for the 95th percentile based on age and gender. Body mass index was the primary efficacy parameter because it takes into account changes in height and body weight, which occur in growing children.

During the study, all patients were instructed to take a multivitamin containing fat- soluble vitamins at least 2 hours before or after ingestion of XENICAL. Patients were also maintained on a well-balanced, reduced-calorie diet that was intended to provide 30% of calories from fat. In addition, all patients were placed on a behavior modification program and offered exercise counseling.

Approximately 65% of patients in each treatment group completed the study.

Following one year of treatment, BMI decreased by an average of 0.55 kg/m2 in the XENICAL-treated patients and increased by an average of 0.31 kg/m2 in the placebo- treated patients (p=0.001).

The percentages of patients achieving ≥ 5% and ≥ 10% reduction in BMI and body weight after 52 weeks of treatment for the intent-to-treat population are presented in Table 7.

Table 7 : Percentages of Patients with ≥ 5% and ≥ 10% Decrease in Body Mass Index and Body Weight After 1-Year Treatment* (Protocol NM16189)

Intent-to-Treat Population
≥ 5% Decrease ≥ 10% Decrease
  XENICAL n Placebo n XENICAL n Placebo n
BMI 26.5% 347 15.7% 178 13.3% 347 4.5% 178
Body Weight 19.0% 348 11.7% 180 9.5% 348 3.3% 180
* Treatment designates XENICAL 120 mg three times a day plus diet or placebo plus diet
Last observation carried forward

Brand Name: Xenical
Generic Name: Orlistat 120 mg
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